HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Styrene → 4-Vinyl-1-cyclohexene
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Styrene | HCID 7501 | — |
| Edukt | Tris(pentafluorophenyl)borane | HCID 582056 | — |
| Katalysator | HCID 178504297 | HCID 178504297 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 4-Vinyl-1-cyclohexene | HCID 7499 | — |
| Produkt | Styrene | HCID 7501 | — |
| Produkt | Vinylcyclohexane | HCID 12757 | — |
Reaktionsschritte
The polymerization conditions of Example 5 were substantially repeated using the bis(diphenyltrimethylsilylmethyl)titanium (II) complex (0.01 M in toluene), and MAO (1.6 M in toluene), dimethylanilinium tetrakispentafluorophenylborate (DMATB) (0.002 M in toluene), or tris(pentafluorophenyl)borane (borane) (0.01 M in toluene) cocatalyst. Styrene monomer, vinylcyclohexane (VCH) or 4-vinylcyclohexene (4-VCH) were polymerized. The resulting styrene polymers possessed crystalline melting points in excess of 260° C., indicating that the polymers were syndiotactic. Molar ratios of reactants and results are contained in Table IV.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05990033 |
| Quelldatensatz | uspto-grants-1999_11 |
| ORD ID | ord-f7a75b960f824b36913ca194edcda800 |
| Quellennotiz | uspto-grants-1999_11 |